Molybdenum oxide 2-D flakes: role of thickness and annealing treatment on the optoelectronic properties of the material

A. Domínguez, A. Dutt, O. de Melo, L. Huerta, G. Santana

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Molybdenum oxide (MoOx) thin films were grown by using a simple, economic and scalable DC Cressington sputtering unit. For thickness measurement with the quartz balance, during the deposition, MoOx density was set to an average value of 5.58 g/cm3 which is the mean density of the two main oxidation states, MoO2 (6.47 g/cm 3) and MoO3, (4.69 g/cm 3), respectively. Afterward, as-deposited samples were annealed in air at 400 °C for 60 min. Then onwards, X-ray diffraction (XRD), field emission scanning microscopy, atomic force microscopy (AFM), UV–visible (UV–Vis) spectroscopy and photoconductivity studies were carried out to investigate the differences appearing in the structural, morphological and optoelectronic properties of the as-deposited and annealed samples. Using AFM and SEM, it was observed a decrease in the average roughness as well in the grain size for thicker samples (after annealing), whereas contrary behavior was found for thinner samples. Presence of α-MoO3 and sub-oxide phases such as β-MoO2 and γ-Mo4O11 with predominance of MoO2 was observed before annealing. XRD and XPS analysis revealed a better crystalline structure for annealed samples in which the MoO3 phase was observed in majority. Depending on the thickness and oxidation states, the electrical behavior of the samples was found to be varied from semimetal to semiconductor. After annealing, all samples shown a semiconductor behavior, with an increase in photoconductivity response for the films with a lower band gap. The aim of the present work is to provide useful information over the control of the morphology and functionality of the thin films with a view to their use for future prospective application especially for the fabrication of hole transport layer in the new generation of solar cells.

Idioma originalInglés
Páginas (desde-hasta)6147-6156
Número de páginas10
PublicaciónJournal of Materials Science
EstadoPublicada - 1 abr. 2018
Publicado de forma externa

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© 2018, Springer Science+Business Media, LLC, part of Springer Nature.


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